Variant report

Variant	nsv970918
Chromosome Location	chr7:101967519-102005026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1245)
CpG islands
(count:672)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102004022-102004495	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102004087-102004234	K562	blood:	n/a	n/a
3	ATF1	chr7:102003979-102004409	K562	blood:	n/a	n/a
4	ATF2	chr7:102003964-102004508	GM12878	blood:	n/a	n/a
5	ATF2	chr7:102003966-102004343	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr7:102004002-102004510	A549	lung:	n/a	n/a
7	ATF3	chr7:102004112-102004430	K562	blood:	n/a	n/a
8	ATF3	chr7:102003901-102004509	A549	lung:	n/a	n/a
9	BACH1	chr7:102004065-102004493	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:102004126-102004439	GM12878	blood:	n/a	n/a
11	BATF	chr7:101995463-101995686	GM12878	blood:	n/a	n/a
12	BATF	chr7:101997851-101998066	GM12878	blood:	n/a	n/a
13	BATF	chr7:101997012-101997266	GM12878	blood:	n/a	n/a
14	BATF	chr7:101977330-101977583	GM12878	blood:	n/a	n/a
15	BATF	chr7:101983890-101984191	GM12878	blood:	n/a	n/a
16	BATF	chr7:102004902-102005484	GM12878	blood:	n/a	n/a
17	BATF	chr7:101982483-101982724	GM12878	blood:	n/a	n/a
18	BATF	chr7:101999193-101999814	GM12878	blood:	n/a	n/a
19	BATF	chr7:101980953-101981449	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:101982462-101982707	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:101975677-101976058	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:101994622-101994770	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:101981186-101981393	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:102003720-102004191	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:102004788-102005191	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101992379-101992526	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:101987225-101987383	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:101983613-101984160	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:101997984-101998246	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:101981081-101981468	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:101982419-101982753	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:101987793-101988042	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:101977204-101977363	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:101999319-101999808	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:102003799-102003974	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:101983901-101984172	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:101990402-101990553	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:101975878-101976049	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:101999465-101999748	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:101996913-101997326	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:101997514-101997663	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:101983656-101983848	GM12878	blood:	n/a	n/a
43	BCL3	chr7:102003976-102004358	A549	lung:	n/a	n/a
44	BCLAF1	chr7:102003953-102004478	GM12878	blood:	n/a	n/a
45	BCLAF1	chr7:102003908-102004427	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:102004102-102004486	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:102004109-102004495	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:102004011-102004495	K562	blood:	n/a	n/a
49	BHLHE40	chr7:101997473-101997748	HepG2	liver:	n/a	n/a
50	BRCA1	chr7:102004018-102004395	Hela-S3	cervix:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101989013-101989063	K562	blood:	n/a
2	chr7:101989013-101989063	K562	blood:	n/a
3	chr7:102004775-102004825	HEEpiC	esophagus:	n/a
4	chr7:101989013-101989063	NHDF-neo	bronchial:	n/a
5	chr7:101989034-101989084	HNPCEpiC	eye:	n/a
6	chr7:102005014-102005064	SKMC	muscle:	n/a
7	chr7:101989013-101989063	MCF10A-Er-Src	breast:	n/a
8	chr7:101989013-101989063	AG04450	lung:	fetal
9	chr7:102004098-102004148	LNCaP	prostate:	n/a
10	chr7:102004098-102004148	BE2_C	brain:	n/a
11	chr7:101998514-101998564	IMR90	lung:	fetal
12	chr7:101999041-101999091	PFSK-1	brain:	n/a
13	chr7:101972144-101972194	AG09319	gingival:	n/a
14	chr7:101989034-101989084	ovcar-3	ovarian:	n/a
15	chr7:101972144-101972194	SKMC	muscle:	n/a
16	chr7:101998514-101998564	AoSMC	blood vessel:	n/a
17	chr7:101991189-101991239	A549	lung:	n/a
18	chr7:101989034-101989084	PrEC	prostate:	n/a
19	chr7:101991189-101991239	PrEC	prostate:	n/a
20	chr7:101999041-101999091	HCM	heart:	n/a
21	chr7:102004775-102004825	HCM	heart:	n/a
22	chr7:101998514-101998564	HAEpiC	amniotic membrane:	n/a
23	chr7:102004098-102004148	HMEC	breast:	n/a
24	chr7:101998514-101998564	HL-60	blood:	n/a
25	chr7:101991189-101991239	HRE	kidney:	n/a
26	chr7:101986487-101986537	HEEpiC	esophagus:	n/a
27	chr7:102004098-102004148	NHDF-neo	bronchial:	n/a
28	chr7:101999041-101999091	AG10803	skin:	n/a
29	chr7:102004098-102004148	Jurkat	blood:	n/a
30	chr7:101989034-101989084	SK-N-SH	brain:	n/a
31	chr7:101986487-101986537	HRCEpiC	kidney:	n/a
32	chr7:101991189-101991239	HUVEC	blood vessel:	n/a
33	chr7:102004298-102004348	NB4	blood:	n/a
34	chr7:101989034-101989084	IMR90	lung:	fetal
35	chr7:101986487-101986537	LNCaP	prostate:	n/a
36	chr7:101998514-101998564	Hela-S3	cervix:	n/a
37	chr7:102004098-102004148	GM12878	blood:	n/a
38	chr7:102004775-102004825	Hela-S3	cervix:	n/a
39	chr7:102004098-102004148	HCF	heart:	n/a
40	chr7:101986487-101986537	GM12892	blood:	n/a
41	chr7:101991189-101991239	GM19239	blood:	n/a
42	chr7:102004098-102004148	PFSK-1	brain:	n/a
43	chr7:102005014-102005064	GM12892	blood:	n/a
44	chr7:102004775-102004825	LNCaP	prostate:	n/a
45	chr7:102004098-102004148	CMK	blood:	n/a
46	chr7:101998514-101998564	PrEC	prostate:	n/a
47	chr7:101991189-101991239	SAEC	small airway:	n/a
48	chr7:101986487-101986537	HepG2	liver:	n/a
49	chr7:102004298-102004348	NT2-D1	testis:	n/a
50	chr7:101991189-101991239	HPAEpiC	pulmonary alveolar:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41465686..41466379-chr7:102004292..102004823,2	NB4	blood:
2	chr7:101962260..101964912-chr7:101971375..101973484,2	MCF-7	breast:
3	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:
4	chr7:101965469..101968383-chr7:101972225..101973731,2	K562	blood:
5	chr7:101928479..101930967-chr7:101967385..101968999,2	MCF-7	breast:
6	chr7:101965469..101968383-chr7:101972225..101973731,2	K562	blood:
7	chr7:101928261..101931030-chr7:101966781..101969545,2	K562	blood:
8	chr7:101927779..101934386-chr7:102001430..102005829,12	MCF-7	breast:
9	chr7:101969853..101972657-chr7:102004064..102005598,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIP1-1	chr7:101995384-101995807	ENSG00000259313.1
2	lnc-PRKRIP1-1	chr7:101993676-101993848	ENSG00000259313.1

No data

Variant related genes	Relation type
ENSG00000228546	TF binding region
ENSG00000200552	TF binding region
ENSG00000239969	TF binding region
SPDYE6	TF binding region
PRKRIP1	TF binding region
ENSG00000170409	TF binding region
ENSG00000228546	CpG island
ENSG00000200552	CpG island
ENSG00000239969	CpG island
SPDYE6	CpG island
PRKRIP1	CpG island
ENSG00000170409	CpG island
ENSG00000188825	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000170409	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000239969	chromatin interactions

Extended variants
information (count: 1186 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565249639	chr7:101967525-101967526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs532525132	chr7:101967528-101967529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116091347	chr7:101967572-101967573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565607263	chr7:101967582-101967583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529831541	chr7:101967653-101967654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201856537	chr7:101967663-101967664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182308030	chr7:101967671-101967672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs803103	chr7:101967698-101967699	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537334337	chr7:101967723-101967724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185139547	chr7:101967739-101967740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570763243	chr7:101967760-101967761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1725578	chr7:101967774-101967775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs534779959	chr7:101967775-101967776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553218453	chr7:101967777-101967778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs803104	chr7:101967821-101967822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191574925	chr7:101967828-101967829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs142515907	chr7:101967830-101967831	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182978811	chr7:101967851-101967852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76322545	chr7:101967958-101967959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138796949	chr7:101967963-101967964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374480066	chr7:101967964-101967965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200350964	chr7:101967973-101967974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554659525	chr7:101968009-101968010	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576421651	chr7:101968051-101968052	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543417811	chr7:101968074-101968075	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551243760	chr7:101968091-101968092	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565213373	chr7:101968113-101968114	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188803192	chr7:101968116-101968117	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146011713	chr7:101968119-101968120	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568804199	chr7:101968121-101968122	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200870766	chr7:101968128-101968129	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs79218117	chr7:101968142-101968143	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs79152666	chr7:101968143-101968144	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192938192	chr7:101968152-101968153	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548306641	chr7:101968154-101968155	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569659361	chr7:101968157-101968158	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530470530	chr7:101968179-101968180	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552222007	chr7:101968183-101968184	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570724448	chr7:101968194-101968195	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376728714	chr7:101968195-101968196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534948565	chr7:101968217-101968218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552868339	chr7:101968218-101968219	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182793890	chr7:101968219-101968220	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544205151	chr7:101968226-101968227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140075575	chr7:101968229-101968230	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187779379	chr7:101968235-101968236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543379096	chr7:101968311-101968312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558564369	chr7:101968323-101968324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577100913	chr7:101968356-101968357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541371899	chr7:101968394-101968395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101944000-101975400	Weak transcription	Right Atrium	heart
2	chr7:101959600-101968000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:101961600-101968000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr7:101961600-101968400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:101961800-101968400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr7:101962000-101973200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:101962400-101967800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:101962800-101970800	Weak transcription	GM12878-XiMat	blood
9	chr7:101962800-101971600	Weak transcription	Primary B cells from cord blood	blood
10	chr7:101963200-101971600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr7:101963800-101971600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:101967800-101968000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:101968000-101968200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr7:101968000-101968400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:101968000-101968600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr7:101968000-101975400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:101968400-101968600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:101968400-101969000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:101968400-101969200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr7:101968400-101969200	Enhancers	Duodenum Mucosa	Duodenum
21	chr7:101968400-101970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr7:101969200-101972200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:101970000-101972000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr7:101970800-101971800	Enhancers	GM12878-XiMat	blood
25	chr7:101971600-101971800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:101971600-101972600	Enhancers	Primary B cells from cord blood	blood
27	chr7:101971600-101972800	Enhancers	Primary B cells from peripheral blood	blood
28	chr7:101971800-101972200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:101971800-101972600	Flanking Active TSS	GM12878-XiMat	blood
30	chr7:101971800-101974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:101972200-101972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:101972200-101972400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr7:101972200-101972600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:101972200-101972600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:101972200-101972800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:101972200-101972800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr7:101972200-101973400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:101972400-101972600	Enhancers	Fetal Kidney	kidney
39	chr7:101972600-101973400	Enhancers	GM12878-XiMat	blood
40	chr7:101972600-101973600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:101972800-101973600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr7:101972800-101973800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:101972800-101980800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr7:101973200-101973600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:101973400-101973600	Enhancers	Fetal Kidney	kidney
46	chr7:101973400-101974200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:101973400-101975200	Weak transcription	GM12878-XiMat	blood
48	chr7:101973600-101974200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr7:101973600-101974800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:101973800-101974000	Enhancers	HUES6 Cell Line	embryonic stem cell

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